Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Daniel J. Rivinoja"'
Autor:
Yi Sing Gee, John H. Ryan, Christopher J. T. Hyland, Daniel J. Rivinoja, Steven M. Wales, Michael G. Gardiner
Publikováno v:
The Journal of Organic Chemistry. 82:13517-13529
A trans-diastereoselective Pd-catalyzed dearomative [3 + 2] cycloaddition between vinylcyclopropane dicarboxylates and 3-nitroindoles has been developed. The reaction provides densely functionalized cyclopenta[b]indolines with versatile vinyl and nit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10e55150b30cbfd275f7c1429e580006
https://doi.org/10.1021/acs.joc.7b02624
https://doi.org/10.1021/acs.joc.7b02624
Publikováno v:
ACS Catalysis. 7:1053-1056
An efficient, diastereoselective synthesis of densely functionalized pyrroloindolines is reported. The reaction proceeds via cycloaddition of a vinylaziridine-derived Pd-stabilized 1,3-dipole to electron-deficient 3-nitroindoles. The reactions give t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f79753a81bd510a536334d1441b18d97
https://doi.org/10.1021/acscatal.6b03248
https://doi.org/10.1021/acscatal.6b03248
Autor:
Michael G. Gardiner, John H. Ryan, Adam G. Meyer, Christopher J. T. Hyland, Steven M. Wales, Melissa J. Bird, Daniel J. Rivinoja
Publikováno v:
Organic letters. 21(12)
Aminobenzaldehydes bearing a pendant 3,5-dinitrophenyl group react thermally with N-substituted α-amino acids to form unprecedented benzoazepine-fused isoindolines. The reaction proceeds via a dearomatization/rearomatization sequence involving an in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc773730709ab65cb6f8f89e0dcf82b4
https://pubmed.ncbi.nlm.nih.gov/31188010
https://pubmed.ncbi.nlm.nih.gov/31188010
Autor:
Daniel J. Rivinoja, Asha M. D’Souza, Christopher J. T. Hyland, Roger J. Mulder, John H. Ryan, Adam G. Meyer, Jonathan M. White
Publikováno v:
Australian Journal of Chemistry. 71:690
A study of the reactivity of a non-stabilised azomethine ylide, derived from N-(methoxymethyl)-N-(trimethylsilylmethyl)benzylamine, with nitro-substituted isatoic anhydrides was undertaken. N-Methyl-4-nitroisatoic anhydride underwent a 1,3-dipolar cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d58466b949843311900b5ed428718369
https://doi.org/10.1071/ch18196
https://doi.org/10.1071/ch18196